WHO monographs on selected medicinal plants - travolekar.ru
WHO monographs on selected medicinal plants - travolekar.ru
WHO monographs on selected medicinal plants - travolekar.ru
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Radix Panacis Quinquefolii<br />
to be drawn. Further randomized c<strong>on</strong>trolled clinical trials with larger<br />
populati<strong>on</strong>s of patients with diabetes and better methodology are needed<br />
before therapeutic recommendati<strong>on</strong>s can be made.<br />
Uses described in traditi<strong>on</strong>al medicine<br />
Used orally as a diuretic, digestive, t<strong>on</strong>ic and a stimulant (5, 6, 23). Used<br />
to enhance stress resistance, and to treat cough, loss of appetite, colic,<br />
vomiting, insomnia, neuralgia, rheumatism and headaches (5, 24).<br />
Experimental pharmacology<br />
Antihyperglycaemic activity<br />
Intraperit<strong>on</strong>eal administrati<strong>on</strong> of an aqueous extract of the root exhibited<br />
significant hypoglycaemic activity in mice with alloxan-induced hyperglycaemia<br />
when administered at a dose of 10 g/kg body weight (bw)<br />
(p < 0.01). Activity-guided fracti<strong>on</strong>ati<strong>on</strong> of the extract led to isolati<strong>on</strong> of<br />
three glycans, the quinquefolans A, B and C, which displayed significant<br />
hypoglycaemic activity (p < 0.01, p < 0.05, p < 0.01, respectively) in normal<br />
mice and in mice with alloxan-induced hyperglycaemia at a dose of 10, 100<br />
and 10 mg/kg bw, of quinquefolans A, B and C, respectively (17).<br />
Antioxidant activity<br />
The antioxidant activity of a root extract c<strong>on</strong>taining 8% ginsenosides<br />
was assessed in the metal chelati<strong>on</strong>, affinity to scavenge 1,1-diphenyl-2-<br />
picrylhydrazyl stable free radical, and peroxyl and hydroxyl free radical<br />
assays. Dissociati<strong>on</strong> c<strong>on</strong>stants (Kd) for the extract to bind transiti<strong>on</strong><br />
metals were of the order of Fe 2+ > Cu 2+ > Fe 3+ and corresp<strong>on</strong>ded to the<br />
affinity to inhibit metal-induced lipid peroxidati<strong>on</strong>. In a metal-free linoleic<br />
acid emulsi<strong>on</strong>, the extract exhibited a significant c<strong>on</strong>centrati<strong>on</strong>dependent<br />
(0.01–10 mg/ml) mitigati<strong>on</strong> of lipid oxidati<strong>on</strong> as assessed by<br />
the amm<strong>on</strong>ium thiocyanate method (p 0.05). The extract also showed<br />
str<strong>on</strong>g 1,1-diphenyl-2-picrylhydrazyl radical scavenging activity up to a<br />
c<strong>on</strong>centrati<strong>on</strong> of 1.6 mg/ml (r 2 = 0.996). The extract also inhibited the<br />
n<strong>on</strong>-site-specific deoxynucleic acid (DNA) strand breakage caused by<br />
Fent<strong>on</strong> agents, and suppressed the Fent<strong>on</strong>-induced oxidati<strong>on</strong> of a 66 Kd<br />
soluble protein obtained from mouse brain over a c<strong>on</strong>centrati<strong>on</strong> range<br />
of 2.0–40.0 mg/ml (25). The free radical scavenging capacity and antioxidant<br />
effects of the c<strong>ru</strong>de d<strong>ru</strong>g appear to be related to the c<strong>on</strong>centrati<strong>on</strong><br />
of ginsenosides Rb1 and Rb2 in the plant (26).<br />
The effect of sap<strong>on</strong>ins, isolated from the root, <strong>on</strong> the oxidati<strong>on</strong> of lowdensity<br />
lipoprotein (LDL) was measured. The potential of the sap<strong>on</strong>ins for<br />
reducing LDL oxidati<strong>on</strong> as well as limiting the ability of oxidized-LDL<br />
231